Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This study aims to compare the clinical results of postoperative wound between Dermabond PRINEOâ„¢(2-octyl Cyanoacrylate adhesive and polyester mesh) and subcuticular suture in simultaneous total knee arthroplasty
There is previous studies over whether or not to use skin adhesive material is superior or inferior to subcuticular suture This study prospectively randomized patients receiving bilateral total knee arthroplasty(TKA). Patients preference and clinical results was investigated in both knee of same patients who received skin adhesive or subcuticular suture in each knee.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dermabond group | Experimental | close capsule using 1-0 vicryl suture material close subq layer using 1-0 and 2-0 bicryl suture material and close skin layer using DERMABONDâ„¢ PRINEOâ„¢ |
|
| Subcuticular group | No Intervention | close capsule using 1-0 vicryl suture material close subq layer using 1-0 and 2-0 bicryl suture material and close skin layer using 3-0 Dermalon with subcuticular suture method |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| DERMABONDâ„¢ PRINEOâ„¢(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) vs subcuticular nylon suture | Procedure | DERMABONDâ„¢ PRINEOâ„¢(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) and subcuticular nylon suture are applied for each knee |
| Measure | Description | Time Frame |
|---|---|---|
| wound Hypertrophy scale at postoperative 6 month | Vancouver scar scale, patient and observer report scar assessment scale | at postoperative 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Skin closure time | Skin closure time for each group | operation day |
| wound complication | postoperative 2 weeks | |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Yong In, MD, PhD | the Catholic Univerisity of Korea Seoul St Mary's hospital | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Seoul St. Mary's Hospital | Seoul | 06591 | South Korea |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Double blind
| wound complication |
| postoperative 6 weeks |
| wound complication | postoperative 3 month |
| wound complication | postoperative 6 month |
| Stitch out time | postoperative 2 weeks |
| Stitch out visual visual analogue scale(VAS) | VAS range from 1 to 10 ( 1means minimal pain 10 means maximal pain) | postoperative 2 weeks |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
Not provided
Not provided